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CompletedNCT01197742SweetheartUpdated Dec 20, 2024

Sweetheart-Register: Risk Management of Diabetics with Acute Myocardial Infarction

An observational study in Diabetes, STEMI and NSTEMI, sponsored by Stiftung Institut fuer Herzinfarktforschung. Completed at 2 sites in Germany. Per ClinicalTrials.gov, last updated 2024-12-20.

Sponsored by Stiftung Institut fuer Herzinfarktforschung · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,772
Sex
All
01

Study summary

The Sweetheart register (Risk management of Diabetics with acute myocardial infarction) documents both the prevalence of pathologic glucose metabolism in consecutive high-risk patients with STEMI and NSTEMI in daily hospital routine as well as the anti-diabetic acute and long-term therapy. Furthermore the register will provide data about the implementation of new guidelines for the interventional and adjuvant medical therapy of STEMI and NSTEMI.

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Conditions studied

  • Diabetes
  • STEMI
  • NSTEMI
  • Myocardial Infarction

Keywords

  • Diabetes
  • STEMI
  • NSTEMI
  • Myocardial infarction
03

In context

Myocardial Infarction

2,744 studies on the registry are indexed under Myocardial Infarction; 418 are open to participants now.

This study's enrollment of 2,772 is above the median of 500 across 983 observational studies indexed under Myocardial Infarction.

Browse Myocardial Infarction studies →

Lead sponsor

Stiftung Institut fuer Herzinfarktforschung is the lead sponsor of 25 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

all consecutive patients with acute (no older than 24 h) ST-Elevation Myocardial infarction or acute (no older than 24 h) Non-ST-Elevation Myocardial infarction.

Inclusion criteria

  • consecutive patients with acute (no older than 24 h) ST-Elevation Myocardial infarction
  • consecutive patients with acute (no older than 24 h) Non-ST-Elevation Myocardial infarction

Exclusion criteria

Exclusion Criteria:

  • missing informed consent
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,772 participants (actual)
06

What researchers measure

Primary outcomes

  1. Documentation of the characteristics consecutive patients with acute STEMI or NSTEMI in daily hospital routine in Germany

    Time frame: 04/01/2007-09/30/2009

Secondary outcomes

  1. Documentation of the fraction of patients with (I) a previous know Diabetes Mellitus (DM) type I and II, (II) a newly diagnosed DM, (III) diagnosed with IFG or IGT for the first time

    Time frame: 04/01/2007-09/30/2009

  2. Documentation of acute invasive and adjuvant medicamentous therapy of STEMI and NSREMI in hospital daily routine in Germany

    Time frame: 04/01/2007-09/30/2009

  3. Documentation of diabetic therapy during the acute phase of a myocardial infarction

    Time frame: 04/01/2007-09/30/2009

  4. Documentation of the hospital mortality, the serious but non-fatal complications (stroke, re-myocardial infarction) and other bleeding complications

    Time frame: 04/01/2007-09/30/2009

  5. Verification of the implementation of a therapy according to the guidelines for STEMI / NSTEMI in daily hospital routine

    Time frame: 04/01/2007-09/30/2009

07

Study locations

2 sites
  • Städ Krankenhaus münchen Schwabing
    München, 80804, Germany
  • Klinikum Nürnberg Süd /Cardiology
    Nürnberg, 90471, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01197742
Lead sponsor
Stiftung Institut fuer Herzinfarktforschung
Collaborators
Sanofi
Responsible party
Sponsor
First posted
Sep 9, 2010
Start date
Apr 20, 2007
Primary completion
Oct 5, 2009
Completion
Oct 5, 2009
Last update
Dec 20, 2024

Study contacts

Anselm K Gitt, MD
study chair · Stiftung Institut für Herzinfarktforschung
Jochen Senges, MD
study chair · Stiftung Institut für Herzinfarktforschung

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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